CA2620554A1 - Treatment of autoimmune diseases - Google Patents

Abstract

Methods of treating various autoimmune diseases, such as multiple sclerosis, peripheral neuritis, optica! neuritis, amylotrophic lateral sclerosis, and uveitis utilizing specific amino alcohol derivatives are provided herein.

Description

TREATMENT OF AUTOIMMUNE DISEASES
Field of the Invention The present invention relates generally to amino alcohols and derivatives thereof, and more specifically to their use to treat particular autoimmune diseases, such as multiple sclerosis, peripheral neuritis, optical neuritis, amyotrophic lateral sclerosis and uveitis.

Background of the Invention Multiple sclerosis is a chronic inflammatory disease of the central nervous system (CNS) with an unknown pathophysiological cause. Clinical manifestations are associated with the infiltration of the central nervous system by immune-competent cells. Specific T cell populations directed towards neuroantigens, such as myelin basic protein, can be demonstrated in the periphery. This suggests the involvement of an autoimmune response in the development of the disease.
Although there is no specific treatment for this T cell-mediated autoimmune disorder, patients receive immunosuppressive therapy including azathioprine and corticosteroids in order to limit the extent of the inflammatory process. Immunosuppressive therapy of multiple sclerosis, however, is only partially effective, and in most cases only offers a delay in disease progression despite anti-inflammatory and immunosuppressive treatment.

Accordingly, there is a need for other therapeutics which are effective in the treatment of multiple sclerosis and other related diseases including those involving T-cell mediated damage to central or peripheral nerve tissue, such as peripheral neuritis, optical neuritis and amyotrophic lateral sclerosis.

It has now been found that an amino alcohol such as disclosed thereafter has a beneficial effect in the treatment of autoimmune diseases such as multiple sclerosis, peripheral neuritis, optical neuritis, amyotrophic lateral sclerosis (Lou Gehrig's disease) or uveitis.

Amino alcohols which can be used according to the invention are compounds of formula 1 R3 ~ x Rs NH2 I I ~CH2OR4 R2 (CH2)~ CH2OR5 wherein X is 0, S, SO or SOZ;

R, is halogen, trihalomethyl, OH, C1_7alkyl, C14alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthyimethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1_4alkylthio, C1_4alkylsulfinyl, C1_4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC,Aalkyf or phenyl-C,_aalkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1_4alkyl or C1_4alkoxy;

R2 is H, halogen, trihalomethyl, C,-4alkoxy, C,_,alkyl, phenethyl or benzyloxy;
R3 H. halogen, CF3, OH, C1_7alkyl, C1_4alkoxy, benzyloxy, phenyl or C,_4alkoxymethyl;
each of R4 and R5, independently is H or a residue of formula (a) P< OR$

O (a) wherein each of R8 and R9, independently, is H or C,,alkyl optionally substituted by halogen; and n is an integer from 1 to 4;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

Rla X. R3a NHRqa R6a R2a (CH2) R II
sa OR7a wherein R,a is halogen, trihalomethyl, C1_4alkyl, C1_4alkoxy, C,-4alkylthio, CI_4alkylsulifinyl, C1_4alkyl-suifonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1_4alkyl, C1_4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C14alkyl, Cl-4alkoxy, CS_4alkylthio or benzyloxy;

R4a is H, C,_qalkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C 1_5acyl;
R5a is H, monohalomethyl, C1_4alkyl, C1-,alkoxy-methyl, CI _4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2_4alkenyl or -alkynyl;

R6a is H or C1_4aikyl;

R7a is H, C1_4alkyl or a residue of formula (a) as defined above, Xa is 0, S, SO or SO2; and na is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof.

With regard to the compounds of formulae (I) and (II), the term "halogen"
encompasses fluorine, chlorine, bromine and iodine. The term "trihalomethyl group" encompasses trifluoromethyl and trichloromethyl. "Cl_7 alkyi" encompasses straight-chained or branched alkyl, e.g. methyl, ethyl, propyl, isopropyl, butyl, t-butyl, pentyl, hexyl or heptyl. The phrase "substituted or unsubstituted phenoxy group" encompasses those that have, at any position of its benzene ring, a halogen atom, such as fluorine, chlorine, bromine and iodine, trifluoromethyl, C1_4alkyl or C,-4alkoxy. The term "aralkyl group" as in "aralkyl group" or "aralkyloxy group" encompasses benzyl, diphenylmethyl, phenethyl and phenylpropyl. Any alkyl moiety as present in "C1_4aikoxy", "Cl_ 4alkylthio", "C,_Qalkylsulfinyl " or "C,Aalkylsulfonyl encompasses straight-chained or branched C,_ 4alkyl, e.g. methyl, ethyl, propyl, isopropyl or butyl. The phrase "substituted or unsubstituted aralkyl group" encompasses those that have, at any position of its benzene ring, a halogen atom, such as fluorine, chlorine, bromine and iodine, trifluoromethyl, lower alkyl having 1-4 carbon atoms, or lower alkoxy having 1-4 carbon atoms.

Preferred compounds of formula I are compounds of formula la R6 O s R3 NH (la) Rz (CH2) el_t~

wherein R2, R3, R4, R5 and n are as defined above; and R6 is hydrogen, halogen, C1_7alkyl, C1_4alkoxy or trifluoromethyl.

Further preferred compounds of formula (Ia) are those wherein R3 is chlorine, e.g., 2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl-propane-1,3-diol and its corresponding phosphate derivative, phosphoric acid mono-2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl-propyl] ester. The phosphoric acid mono-2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl-propyl] ester can be prepared enantiomerically pure by the procedures described in WO 2005/021503.

Preferred compounds of formula II are compounds of formula (Ila) R3a NH Ila (CH2) R OR7a R2a 5a wherein Y is 0 or S; and R2a, R3a, R5a, R7a and na are as defined above.

Preferred compounds of formula (Ila) are those wherein R3 is chlorine, e.g., 2-amino-4-[4-(3-benzyloxyphenyithio)-2-chlorophenyl]-2-mekhylbutane-l-ol; the corresponding phosphoric acid mono-2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylbutyl]
ester; 2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethylbutane-l-ol; and the corresponding phosphoric acid mono-2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethylbutyl] ester.

Compounds of formulae I and I[ are known and are disclosed e.g. in W003/029205, WO
03/029184 and W0041026817, respectively, the phosphorylated derivatives being disclosed e.g.
in W004/074297, the contents of which being incorporated herein by reference intheir entirety.
Compounds of formulae I and 11 may be prepared as disclosed in above cited references.

Phosphorylated derivatives of compounds of formula (I), e.g., phosphoric acid mono-2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl-propyl] ester, can be prepared utilizing the procedures for synthesizing phosphorylated compounds described e.g., in WO
2005/021503 (see, e.g., pages 11 and 12). Optically active compounds of structural formula (I) and phosphorylated derivatives thereof, in particular of formula (1a) can be prepared in high purity utilizing the procedure described, e.g., in Hinterding et al., Synthesis, Vol. 11, pp.1667-1670 (2003). As an example, an optically active compound of structural formula (Ia), phosphoric acid mono-2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]ethyl-propyl] ester, can be prepared as described in the scheme below utilizing the procedures of Hinterding et al. (2003) supra.

~
~ a) Boc-anhydride s ~ ci ~ ~ o s ci I
~ o oH b) o Nitrobenzoylchloride N
NHz 0zN
Ho c) Acetonedimethylacetale o \

o s ci d) KZC03 s ci 2N 0 Q ~~ e) Tetrazole f) H202 N~
o -P/ o IkpP, p X

a) 1 equivalent of compound 1 and 1.2 equivalents Boc-anhydride in dioxane/acetonitrile or DMF/water (depends on solubility) + 1.2 equivalents NaOH 1 M in water (RT, overnight).

b) 1 equivalent of step a), 1.5 equivalents 2-nitrobenzoylchloride and 1.6 equivalents pyridine in CH2CI2 (RT, overnight).

c) 1 equivalent of step b), 3 equivalents acetonedimethylacetale and 0.1 equivalents p-TsOH=H20 in toluene (95 C, 3 hours).

d) 1 equivalent of step c) and 0.075 equivalents K2CO3 (powder) in MeOHITHF
(1/1) (RT, 4 hours).

e) 1 equivalent of step a), 6 equivalents tetrazole (recrystallized from toluene or 0.45 M in CH3CN) and 2 equivalents di-t-butyldiethylphosphoramidite in dry THF (RT, 3 hours).

f) 5 equivalents H202 (30%) directly into the reaction mixture of step e) (0 C, 1 hour).
Isolation: the reaction mixture is quenched with sodium thiosulfate (saturated in water) and extracted with ethyl acetate (3 x).

O S i~ CI

O
N~ chiral separation O /Ih O~P~ O O ChiralcelOD-H
O O

I
0_1"0 5 Cl O S CI
O
N-O
p11 /
~O P\
OO O O O
O O O //O
TFA/H20 9515 (room temp) min CL'O S CI
I i O S C cl OH I
' _OH NH2 NHz O
O HO1P~
HO-p~

Phosphoric acid mono-{(S)-2-amino-4- Phosphoric acid mono-{(R)-2-amino-4-[4-(3-benzyloxy-phenylsulfanyl)-2-chloro- [4-(3-benzyloxy-phenylsulfanyl)-2-chloro-phenyl]-2-hydroxymethyl-butyl}ester phenyl]-2-hydroxymethyl-butyl}ester The compounds of formulae II and Ila, .e.g., 2-amino-4-(4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-methylbutane-l-ol and 2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethylbutane-l-ol can be prepared as described e.g., in EP 1 548 003 Al.
Preparation of such compounds of formulae Ii and Ila in high optical purity, can be prepared by the procedures described e.g., in Hinterding et al. (2003), supra; and Hinterding et al., Tetra Lett, Vol. 43, No. 45, pp. 8095-8097 (2002). Optically active phosphate derivatives of compounds of structural formulae II and Ila, e.g., phosphoric acid mono-2-amino-4-[4-(3-benzyloxyphenyEthio)-2-chlorophenyl]-2-methyibutyl] ester and phosphoric acid mono-2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethylbutyl] ester can be prepared in high purity as described in Hinterding et al.
(2003), supra.

The compounds of formulae I and II may exist in free or salt form, or as a hydrate. Examples of pharmaceutically acceptable salts of the compounds of the formulae I and II
include salts with inorganic acids, such as hydrochloride and hydrobromide, salts with organic acids, such as acetate, trifluoroacetate, citrate, tartrate, methanesulfonate salts.

When the compounds of formulae I and 11 have one or more asymmetric centers in the molecule, such compounds are to be understood as embracing the various optical isomers, as well as racemates, diastereoisomers and mixtures thereof.

In accordance with the particular findings of the present invention, there is provided 1.1 A method for treating an autoimmune disease selected from the group consisting of peripheral neuritis, optical neuritis, amyotrophic lateral sclerosis and uveitis in a subject in need of such treatment, which method comprises administering to the subject an effective amount of a compound of formula I or II or a pharmaceutically acceptable salt thereof.

1.2 A method for treating multiple sclerosis in a subject in need of such treatment, which method comprises administering to the subject an effective amount of a compound of formula I
wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or C1-4alkyl, or a pharmaceutically acceptable salt thereof.

1.3 A method for alleviating or delaying progression of the symptoms of a demyelinating disease, e.g. multiple sclerosis or Guillain-Barre syndrome, in a subject in need of such treatment, which method comprises administering to the subject an effective amount of a compound of formula I wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof.

1.4 A method for slowing the progression of physical disability or reducing the rate of clinical relapses in a subject with established multiple sclerosis, which method comprises administering to the subject an effective amount of a compound of formula I wherein each of R4 and R5 is H or a compound of formula 11 wherein R7a is H or Cz 4alkyl, or a pharmaceutically acceptable salt thereof.

1.5 A method for reducing the development of brain lesions or the progression of central nervous system demyelination in a subject with suspected or established multipie sclerosis, which method comprises administering to the subject an effective amount of a compound of formula I
wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or CI_4alkyl, or a pharmaceutically acceptable salt thereof.

1.6 A method for preventing or delaying a second demyelinating event, e.g. a second attack of multiple sclerosis, in a subject in need thereof, which method comprises administering to the subject an effective amount of a compound of formula I wherein each of R4 and R5 is H or a compound of formula Il wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof.

1.7 A method for treating optic neuritis in a subject in need thereof, which method comprises administering to the subject an effective amount of a compound of formula I
wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or C1-4alkyl, or a pharmaceutically acceptable salt thereof.

Optic neuritis may be a first symptom associated with a high risk of clinically definite multiple sclerosis.

2.1 A compound of formula I or II or a pharmaceutically acceptable salt thereof, for use in a method according to 1.1 above.

2.2 A compound of formula I wherein each of R4 and R5 is H or a compound of formula II
wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof, for use in any one of the methods according to 1.2 to 1.7 above.

3.1 A pharmaceutical composition for use in a method according to 1.1 above, comprising a compound of formula I or II or a pharmaceutically acceptable salt thereof, together with one or more pharmaceutically acceptable diluents or carriers therefor.

3.2 A pharmaceutical composition for use in any one of the methods according to 1.2 to 1.7 above, comprising a compound of formula I wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof, together with one or more pharmaceutically acceptable diluents or carriers therefor.

4.1 Use of a compound of formula I or II or a pharmaceutically acceptable salt thereof in the preparation of a medicament for use in a method according to 1.1 above.

4.2 Use of a compound of formula I wherein each of R4 and R5 is H or a compound of formula II
wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for use in any one of the methods according to 1.2 to 1.7 above.

The term "effective amount" refers to an amount of a compound of formula I or II which, when administered to the patient, is effective to treat an autoimmune disease, such as multiple sclerosis, peripheral neuritis, optical neuritis, amyotrophic lateral sclerosis (Lou Gehrig's disease) and uveitis. With respect to treatment of an autoimmune disease this includes a reduction of symptoms of the disease, and any other indicators known in the art which show the treatment of the autoimmune disease.

Utility of the compounds of formulae I and II in treating the diseases, disorders or conditions as hereinabove specified, may be demonstrated in animal test methods as well as in clinic, for example in accordance with the methods hereinafter described. The most widely used animal model for multiple sclerosis is experimental autoimmune encephalomyelitis (EAE), based on shared histopathological and clinical features with the human disease.

Methods Animal models: The monophasic model of acute experimental autoimmune encephalomyelitis (EAE) and the chronic relapsing form are considered to be instructive animal models for multiple sclerosis. EAE can be induced in susceptible animals by a single injection of CNS tissue or MBP
emulsified in complete Freund's adjuvant into the base of the tail. A
monophasic acute paralytic disease appears in susceptible rat strains, e.g., Lewis, Wistar rat, about 8-11 days post-sensitization. The symptomatic rats recover within the following 7 days, but in other species the attack is usually lethal. In the chronic relapsing disease models rats undergo one to three relapses following the acute disease bout. These relapses are usually from very mild to severe and are observed within 20-100 days after the acute bout.

1. Acute EAE model Female Lewis rats are immunized by intracutaneous injection in the hind-paws with 0.1 mL of a mixture of guinea pig spinal cord and complete Freund's adjuvant [Difco H37 RA] (3.5 g guinea pig spinal cord + 3.5 mL 0.9% NaCI + 105 mg M. tuberculosis [Difco H37 RAI + 7 mL CFA (Difco H37 RA). Five-ten rats per group are used and somatic symptoms are judged daily on a scale of 0-3. The number of diseased animals as well as the time of onset of the disease is recorded.
Test compounds, e.g. a compound of formula I or II, e.g. [Compound A: 2-amino-2-[4-(3-benzyloxyphenylthio)-2-chlorophenyi]ethyl-propane-1,3-diol; Compound B: (R)-2-amino-4-[4-(3-benzyfoxyphenylthio)-2-chlorophenyl]-2-methylbutane-l-ol; and Compound C: (R)-2-amino-4-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-2-ethylbutane-1-o!) are administered daily from days 0-13 days by oral gavage. The statistical significance between treated and untreated groups is analyzed on each day using ANOVA analysis of variance followed by Dunn's multiple comparisons. In the absence of drug treatment symptoms of the disease (paralysis of the tail and both hind legs) usually develop within 8-11 days.

Clinical grades:
1= loss of tail tonicity 2= weakness of one or both hind legs, or mild ataxia 3 = severe ataxia or paralysis accompanied by urinary incontinence As shown in Table 1 below, Compounds A, B and C lead to prevention of disease symptoms when administered at doses between 0.1 and 10 mg/kg/day in this model.
Table 1 Compound Dose Number of Animals with EAE/total First symptoms mg/kg p.o. Day 12 Mean score in Day 14 on day control Control - 5/ 5 severity = 2.8 9 CompoundA 0.1 0/5 3/4 9 0.3 0/5 1 /5 14 1 0/5 0/5 >14 Control - 5/ 5 severity = 3 10 Compound B 1 0/5 0/5 > 14 Compound C 1 0/5 0/5 > 14 Severity = clinical grades 0-3 As shown in Figure 1, Compound A prevents disease symptoms when administered orally at doses between 0.1 and 10mg/kg/day in this model Figure 1 shows the dose response effect of Compound A on prevention of disease symptoms in the acute EAE model.

2. Chronic-Relapsing EAE Model Chronic-relapsing EAE is induced by injecting an emulsion of guinea pig spinal cord in complete Freund's adjuvant in the hind paws of Lewis rats. Six to ten rats per group are used and somatic symptoms are judged daily on a scale of 0-3. The number of diseased animals as well as the time of onset of the disease is recorded. Treatment with the test compound, e.g. a compound of formula I or 11, e.g. Compound A as defined supra, is started on day 16 (after first disease bout) and continued until day 31. The statistical significance between treated and untreated groups is analyzed on each day using ANOVA analysis of variance followed by Dunn's multiple comparisons. In the absence of drug treatment 80-100% of the sensitized rats show clinical relapses during the first 40 days following immunization.

Clinical grades:
1 = loss of tail tonicity 2 = weakness of one or both hind legs, or mild ataxia 3 = severe ataxia or paralysis accompanied by urinary incontinence As shown in Figure 2, Compound A prevents clinical relapses when administered orally at a doses of 0.3mg/kg/day in the chronic relapsing EAE model. Figure 2 shows the effect of Compound A on prevention of disease symptoms in the chronic relapsing EAE model.

It is expected that similar results obtained with Compound A would be observed for Compounds B
and C.

3. Chronic EAE Model Induction of AEA in DA rat is induced as described by Lorentzen et al, 1995, J. Neuroimmunol.;
63(2):193-205 and Adelmann et ai, 1995, J. Neuroimmunol.; 63(1):17-27.
Briefly, rats are immunized with a mixture of DA rat brain and DA rat and bovine spinal cord homogenate supplemented with 0.02 g/ml purified recombinant rat MOG protein. The mixture is homogenized and then mixed 1:1 with complete Freund's adjuvant containing 4 mg/mi M.
tuberculosis H37RA(CFA). The resultant mixture is then homogenized using a Polytron PT3100 homogenizer (Kinematica, Lucerne, Switzerland). Rats are then injected subcutaneously at the dorsal root of tail with a single injection of 200 l antigen/CFA. The resultant chronic disease is evaluated using numeric scale of progressive paralysis: 0, no paralysis; 1, loss of tail tonicity; 2, hindlimb weakening or ataxia; 3, hindlimb paralysis with or without urinary incontinence; 4, hindlimb and forelimb paralysis; 5, moribund or death. Clinical scores are evaluated on a daily basis, while body weight is determined every other day. At the peak of clinical disease, prior to treatment, animal groups are rearranged such that the clinical disease scores are comparable.
Treatment of animals begins at the peak clinical disease on the 12th day and continues daily the 33rd day post-immunization (total 22 days). The test compound or vehicle (for the control groups) is administered orally daily.

In this assay, Compound A administered orally at a dose of 0.3, 0.1 or 0.03 mglkg/d effectively inhibits chronic EAE. Statistically analysis demonstrates significant reduction in clinical disease at each dose of Compound A compared to that of the vehicle group.

Clinical Trial Suitable clinical studies are, e.g., open-label, dose-escalation or randomized, double-blind studies in patients with the aforementioned demyelinating diseases, multiple sclerosis, peripheral neuritis, optical neuritis, amyotrophic lateral sclerosis and uveitis. The beneficial effects on these autoimmune diseases, can be determined directly through the results of these studies which are known as such to a person skilled in the art. Such studies may also be suitable to compare the effects of a monotherapy using compounds of formula I or II as active ingredient and a combination of such compounds with a second drug substance.
For example, 50 patients with relapsing-remitting multiple sclerosis receive the test compound, e.g a compound of formula I or II, preferably a compound of formula I wherein each of R4 and R5 is H
or a compound of formula II wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof, at a daily dosage of 0.5 to 50 mg p.o. The general clinical state of the patient is investigated weekly by physical and laboratory examination. Disease state and changes in disease progression are assessed every 2 months by radiological examination (MRI) and physical examination. Initially patients receive treatment for 2 to 6 months.
Thereafter, they remain on treatment for as long as their disease does not progress and the drug is satisfactorily tolerated.
Main variables for evaluation: Safety (adverse events), standard serum biochemistry and hematology, magnetic resonance imaging (MRI).

Instead of patients with relapsing-remitting multiple sclerosis, patients having a first isolated, well-defined neurologic event consistent with demyelination and e.g. involving the optic nerve (unilateral optic neuritis), spinal cord (e.g. incomplete transverse myelitis) or brain stem or cerebellum (brain-stem or cerebellar syndrome) confirmed on ophthalmologic or neurologic examination, may undergo clinical treatment with a compound of formula I or 11, preferably a compound of formula I wherein each of R4 and R5 is H or a compound of formula II wherein R7a is H or C1_4alkyl, or a pharmaceutically acceptable salt thereof.

Daily dosages required in practicing the method of the present invention will vary depending upon, for example, the compound used, the host, the mode of administration and the severity of the condition to be treated. A preferred daily dosage range is about from 0.1 to 100 mg as a single dose or in divided doses. Suitable daily dosages for patients are on the order of from e.g. 0.1 to 50 mg p.o. The compound may be administered by any conventional route, in particular enterally, e.g. orally, e.g. in the form of tablets, capsules, drink solutions, nasally, pulmonary (by inhalation) or parenterally, e.g. in the form of injectable solutions or suspensions.
Suitable unit dosage forms for oral administration comprise from ca. 0.1 to 30 mg, usualty 0.25 to 30 mg active ingredient, e.g. from about 0.1 -- 5 mg, together with one or more pharmaceutically acceptable diluents or carriers therefore.

Compounds of formula I or II may be administered by any conventional route, in particular, enterally, e.g., orally, e.g., in the form of tablets or capsules, or parenterally, e.g., in the form of injectable solutions or suspensions, topically, e.g., in the form of lotions, gels, ointments or creams, or in a nasal or a suppository form. Phosphate derivatives of the compounds of formula I
or II are preferably administered parenterally. Pharmaceutical compositions comprising such compounds in free form or in pharmaceutically acceptable salt form in association with at least one pharmaceutical acceptable carrier or diluent may be manufactured in conventional manner by mixing with a pharmaceutically acceptable carrier or diluent.

The compounds of formula I or II may be administered in free form or in pharmaceutically acceptable salt form, e.g., as indicated above. Such salts may be prepared in conventional manner and exhibit the same order of activity as the free compounds.

Compounds of formula I or II may be administered as the sole active ingredient or in conjunction with, e.g., as an adjuvant to, other drugs, e.g., immunosuppressive or immunomodulating agents or other anti-inflammatory agents for the treatment of the afore-mentioned autoimmune disorders.
For example, the compounds may be used in combination with interferons, e.g., pegylated or non-pegylated a-interferons, P-interferons or y-interferons, e.g., administered by subcutaneous, intramuscular or oral routes; an altered peptide ligand, such as Glatiramer, e.g., in the acetate form; monoclonal antibodies to various T-cell surface markers, e.g.
natalizumab (ANTEGRENO) or alemtuzumab; an ascomycin having immunosuppressive properties, e.g., ABT-281, ASM981, etc.; a steroid, e.g. methylprednisolone, prednisone or dexamethasone; a corticosteroid;
cyclophosphamide; azathioprine; methotrexate; mitoxantrone; leflunomide;
mizoribine;
mycophenolic acid; mycophenolate mofetil; 15-deoxyspergualine or an immunosuppressive homologue, analogue or derivative thereof; immunosuppressive monoclonal antibodies, e.g., monoclonal antibodies to leukocyte receptors, e.g., MHC, CD2, CD3, CD4, CD7, CD8, CD25, CD28, CD40, CD45, CD58, CD80, CD86 or their ligands; other immunomodulatory compounds, e.g., a recombinant binding molecule having at least a portion of the extracellular domain of CTLA4 or a mutant thereof, e.g., an at least extracellular portion of CTLA4 or a mutant thereof joined to a non-CTLA4 protein sequence, e.g., CTLA41g, e.g., designated ATCC
68629, or a mutant thereof, e.g., LEA29Y; adhesion molecule inhibitors, e.g., LFA-1 antagonists, ICAM-1 or -3 antagonists, VCAM-4 antagonists or VLA-4 antagonists; cathepsin S inhibitors;
mTOR inhibitors, e.g., rapamycin, 40-0-(2-hydroxyethyl)-rapamycin, CC1779 or ABT578;
calcineurin inhibitors, e.g., cyclosporin A, FK 506 or ISA Tx247.

Where compounds of formula I or III are administered in conjunction with other immunosuppressivelimmunomodulatory or anti-inflammatory therapy, dosages of the co-administered immunosuppressant, immunomodulatory or anti-inflammatory compound will of course vary depending on the type of co-drug employed, e.g., whether it is a steroid or a calcineurin inhibitor, on the specific drug employed, on the condition being treated and so forth.

Accordingly, in yet a further aspect, the invention provides:

5. A method as defined above comprising co-administration, e.g. concomitantly or in sequence, of a#herapeutically effective non-toxic amount of a compound of formula I or II or a pharmaceutically acceptable salt thereof, e.g. a compound of formula I wherein each of R4 and R5 is H or a compound of formula Ii wherein R7a is H or C1_4alkyl, and at least a second drug substance, e.g. as indicated above.

6. A pharmaceutical combination, e.g. a kit, comprising a) a first agent which is a compound of formula I or II or a pharmaceutically acceptable salt thereof, e.g. a compound of formula I wherein each of R4 and R5 is H or a compound of formula II wherein R71 is H or C1_4alkyl, in free form or in pharmaceutically acceptable salt form, and b) at least a second drug substance, e.g. as indicated above. The kit may comprise instructions for its administration.

The terms "co-administration" or "combined administration" or the like as utilized herein are meant to encompass administration of the selected therapeutic agents to a single patient, and are intended to include treatment regimens in which the agents are not necessarily administered by the same route of administration or at the same time.

The term "pharmaceutical combination" as used herein means a product that results from the mixing or combining of more than one active ingredient and includes both fixed and non-fixed combinations of the active ingredients. The term "fixed combination" means that the active ingredients, e.g., a compound of the invention and a second drug substance, are both administered to a patient simultaneously in the form of a single entity or dosage. The term "non-fixed combination" means that the active ingredients, e.g., a compound of the invention and a second drug substance, are both administered to a patient as separate entities either simultaneously, concurrently or sequentially with no specific time limits, wherein such administration provides therapeutically effective levels of the 2 compounds in the body of the patient. The latter also applies to cocktail therapy, e.g., the administration of 3 or more active ingredients.

Claims (14)

1. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H or a residue of formula (a) wherein each of R8 and R9, independently, is H or C1-4alkyl optionally substituted by halogen; and n is an integer from 1 to 4;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;

R7a is H, C1-4alkyl or a residue of formula (a) as defined above, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for the treatment of peripheral neuritis, optic neuritis, amyotrophic lateral sclerosis or uveitis.

2. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for treating multiple sclerosis.

3. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for alleviating or delaying progression of the symptoms of a demyelinating disease.

4. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;

each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for slowing the progression of physical disability or reducing the rate of clinical relapses in a subject with established multiple sclerosis.

5. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for reducing the development of brain lesions or the progression of central nervous system demyelination in a subject with suspected or established multiple sclerosis.

6. Use of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, for preventing or delaying a second demyelinating event.

7. Use of a compound of formula I

wherein X is O, S, SO or SO2, R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohatomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;

R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for use according to any one of claims 2 to 6.

8. A pharmaceutical composition for use according to any one of claims 2 to 6, comprising a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;
R2is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-6acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;
R6a is H or C1-4alkyl;

R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof, together with one or more pharmaceutically acceptable diluents or carriers therefor.

9. Use of a compound of formula I or II as defined in claim 1 or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for use in the treatment of peripheral neuritis, optic neuritis, amyotrophic lateral sclerosis or uveitis.

10. A pharmaceutical composition for use in the treatment of peripheral neuritis, optic neuritis, amyotrophic lateral sclerosis or uveitis, comprising a compound of formula I
or II as defined in claim 1 or a pharmaceutically acceptable salt thereof, together with one or more pharmaceutically acceptable diluents or carriers therefor.

11. A method for treating an autoimmune disease selected from the group consisting of peripheral neuritis, optic neuritis, amyotrophic lateral sclerosis and uveitis, in a subject in need of such treatment, which method comprises administering to the subject an effective amount of a compound of formula I or II as defined in claim 1 or a pharmaceutically acceptable salt thereof.

12. A method for treating any disease, disorder or condition as defined in any one of claims 2 to 6, comprising administering to the subject an effective amount of a compound of formula I

wherein X is O, S, SO or SO2;

R1 is halogen, trihalomethyl, OH, C1-7alkyl, C1-4alkoxy, trifluoromethoxy, phenoxy, cyclohexylmethyloxy, pyridylmethoxy, cinnamyloxy, naphthylmethoxy, phenoxymethyl, CH2-OH, CH2-CH2-OH, C1-4alkylthio, C1-4alkylsulfinyl, C1-4alkylsulfonyl, benzylthio, acetyl, nitro or cyano, or phenyl, phenylC1-4alkyl or phenyl-C1-4alkoxy each phenyl group thereof being optionally substituted by halogen, CF3, C1-4alkyl or C1-4alkoxy;

R2 is H, halogen, trihalomethyl, C1-4alkoxy, C1-7alkyl, phenethyl or benzyloxy;
R3 H, halogen, CF3, OH, C1-7alkyl, C1-4alkoxy, benzyloxy, phenyl or C1-4alkoxymethyl;
each of R4 and R5, independently is H;

or a pharmaceutically acceptable salt thereof, or a compound of formula II

wherein R1a is halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4alkylsulifinyl, C1-4alkyl-sulfonyl, aralkyl, optionally substituted phenoxy or aralkyloxy;

R2a is H, halogen, trihalomethyl, C1-4alkyl, C1-4alkoxy, aralkyl or aralkyloxy;
R3a is H, halogen, CF3, C1-4alkyl, C1-4alkoxy, C1-4alkylthio or benzyloxy;

R4a is H, C1-4alkyl, phenyl, optionally substituted benzyl or benzoyl, or lower aliphatic C1-5acyl;
R5a is H, monohalomethyl, C1-4alkyl, C1-4alkoxy-methyl, C1-4alkyl-thiomethyl, hydroxyethyl, hydroxypropyl, phenyl, aralkyl, C2-4alkenyl or -alkynyl;

R6a is H or C1-4alkyl;
R7a is H or C1-4alkyl, X a is O, S, SO or SO2; and n a is an integer of 1 to 4;

or a pharmaceutically acceptable salt thereof.

13. A method according to claim 11 or 12, comprising co-administration to the subject, concomitantly or in sequence, of at least a second drug.

14. A combination for use according to any one of claims 1 to 6 comprising a) a compound of formula I or II as defined in claim 1 or 2 or a pharmaceutically acceptable salt thereof, and b) at least a second drug.